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Edwards TAVR Receives FDA Approval for Patients With Asymptomatic Severe Aortic Stenosis

May 01, 2025 by
BUSINESS WIRE

Edwards TAVR Receives FDA Approval for Patients With Asymptomatic Severe Aortic Stenosis

HighLife granted US FDA Breakthrough Device Designation for its TMVR solution

Apr 07, 2025 by
HighLife

HighLife granted US FDA Breakthrough Device Designation for its TMVR solution

Abbott Initiates New Intravascular Lithotripsy Clinical Trial to Improve Outcomes in Patients with Coronary Artery Disease

Mar 24, 2025 by
PRNewswire

Abbott Initiates New Intravascular Lithotripsy Clinical Trial to Improve Outcomes in Patients with Coronary Artery Disease

Teleflex to Acquire BIOTRONIK’s Vascular Intervention Business

Feb 27, 2025 by
GLOBE NEWSWIRE

Teleflex to Acquire BIOTRONIK’s Vascular Intervention Business

Medtronic to Distribute Contego’s Carotid and Peripheral Vascular Portfolio in the United States

Jan 13, 2025
Medtronic to Distribute Contego’s Carotid and Peripheral Vascular Portfolio in the United States

CMS Initiates NCA on Renal Denervation for Uncontrolled Hypertension

Jan 13, 2025
CMS Initiates NCA on Renal Denervation for Uncontrolled Hypertension

Corvia Atrial Shunt Receives CE Mark Certification Under EU MDR

Jan 10, 2025
Corvia Atrial Shunt Receives CE Mark Certification Under EU MDR

Boston Scientific Announces Acquisition Agreement for Bolt Medical

Jan 08, 2025
Boston Scientific Announces Acquisition Agreement for Bolt Medical

Stryker announces definitive agreement to acquire Inari Medical, Inc., providing entry into high-growth peripheral vascular segment

Jan 06, 2025 by
GLOBE NEWSWIRE

Stryker announces definitive agreement to acquire Inari Medical, Inc., providing entry into high-growth peripheral vascular segment

FDA Issues Draft Guidance for Development of AI-Enabled Medical Devices

Jan 06, 2025
FDA Issues Draft Guidance for Development of AI-Enabled Medical Devices

Best Vascular/Novoste Celebrates the 24th Anniversary of Vascular Brachytherapy Approval & Use of by US FDA

Nov 12, 2024 by
EINPresswire

Best Vascular/Novoste Celebrates the 24th Anniversary of Vascular Brachytherapy Approval & Use of by US FDA

Recor Medical Announces CMS Grant of Transitional Pass-Through (TPT) Payment for Recor’s Paradise Ultrasound Renal Denervation System for the Treatment of Uncontrolled Hypertension

Nov 01, 2024 by
Recor

Recor Medical Announces CMS Grant of Transitional Pass-Through (TPT) Payment for Recor’s Paradise Ultrasound Renal Denervation System for the Treatment of Uncontrolled Hypertension

Structural heart specialist Transmural Systems strengthens board as it prepares for rapid growth

Oct 15, 2024
Structural heart specialist Transmural Systems strengthens board as it prepares for rapid growth

Pi-Cardia Receives FDA Market Clearance for ShortCut™

Sep 30, 2024 by
BUSINESS WIRE

Pi-Cardia Receives FDA Market Clearance for ShortCut™

ESC Guidelines Recognizing the Importance of Imaging-Guided Percutaneous Coronary Intervention for Complex Lesions

Aug 30, 2024
ESC Guidelines Recognizing the Importance of Imaging-Guided Percutaneous Coronary Intervention for Complex Lesions

Teleflex’s Ringer Perfusion Balloon Catheter Receives FDA Clearance

Aug 06, 2024 by
CARDIAC INTERVENTIONS TODAY

Teleflex’s Ringer Perfusion Balloon Catheter Receives FDA Clearance

Edwards Lifesciences to Acquire Innovalve

Jul 15, 2024 by
BUSINESS WIRE

Edwards Lifesciences to Acquire Innovalve

HighLife welcomes Stefan Pilz as new Chief Executive Officer

Jul 09, 2024
HighLife welcomes Stefan Pilz as new Chief Executive Officer

Alnylam Reports Positive Topline Results from HELIOS-B Phase 3 Study of Vutrisiran, Achieving Statistical Significance on Primary and All Secondary Endpoints in Both Overall and Monotherapy Population

Jun 24, 2024 by
BUSINESS WIRE

Alnylam Reports Positive Topline Results from HELIOS-B Phase 3 Study of Vutrisiran, Achieving Statistical Significance on Primary and All Secondary Endpoints in Both Overall and Monotherapy Populations

Cordis Announces Positive 24-Month Results from Superficial Femoral Artery Study, Confirming Sustained Benefits of SELUTION SLR™ (sustained limus release) Drug-Eluting Balloon in Complex Patients

Jun 18, 2024 by
PRNewswire

Cordis Announces Positive 24-Month Results from Superficial Femoral Artery Study, Confirming Sustained Benefits of SELUTION SLR™ (sustained limus release) Drug-Eluting Balloon in Complex Patients

1-20 of 64 results
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